Tiny study hunts for hidden genes behind immune failures
NCT ID NCT03414528
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study analyzed DNA from 9 patients with primary immune deficiencies whose genetic cause was unknown. Researchers used whole exome or genome sequencing to look for new mutations that might explain their condition. The goal was to identify new inborn errors of immunity, which could improve understanding and diagnosis of these rare disorders.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- What this could lead to
- If successful, this could help identify new genetic causes of immune disorders, potentially leading to better diagnosis and future treatments.
- What could go wrong
- This is a very small, completed study with only 9 participants, so findings may not apply broadly. It is exploratory and does not test any treatment.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University Children's Hospital Zurich
Zurich, 8032, Switzerland
More trials for these conditions
Other studies related to the condition(s) this trial covers.